oomnia RTSM - 2026 Pricing, Features, Reviews & Alternatives

oomnia RTSM is a comprehensive randomization and trial supply management system that functions as an integral component of a unified clinical trial ecosystem. The system automates treatment allocation directly within electronic case report forms, tracks investigational product inventory across sites, and delivers real-time insights to prevent supply shortages. Operating as part of a single unified platform, oomnia RTSM eliminates the need for integration between separate systems, allowing clinical trial professionals to manage studies from one centralized hub that combines electronic data capture and randomization functionality.

The platform offers instant randomization capabilities that enable users to randomize participants, verify investigational medicinal product availability, assign the correct kit, and allocate study arms with a single click. oomnia RTSM supports various standard randomization approaches and algorithms while maintaining the flexibility to develop and validate non-standard approaches. The system extends beyond traditional participant randomization to accommodate complex scenarios including device or image reader randomization through its flexible data model design. Smart supply logistics features include automated notifications when inventory levels drop or products near expiry, dynamic expiry protection that blocks delivery of expired products, and instant accurate kit assignment that eliminates manual checks.

oomnia RTSM streamlines clinical operations through its unified database model that enables direct communication between electronic data capture and randomization systems, eliminating the need for reconciliation and reducing manual work. The platform provides comprehensive oversight of clinical operations in real time, allowing users to focus on critical elements and prevent protocol deviations. With customizable randomization setup options, users can easily configure methods such as stratified, block, or dynamic randomization and upload lists to tailor the randomization process to specific trial designs. The system also features versatile data export capabilities that convert reports for efficient analysis and stakeholder collaboration while maintaining full protocol adherence through its compliance mechanisms.